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INSTITUT KATHAROS

⚠️ Moderate Risk

FEI: 3014034786 • Aix En Provence • FRANCE

FEI

FEI Number

3014034786

📍

Location

Aix En Provence

🇫🇷

Country

FRANCE
🏢

Address

Boulevard De La Republi, , Aix En Provence, , France

Moderate Risk

FDA Import Risk Assessment

28.6
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
6
Unique Violations
7/10/2018
Latest Refusal
7/10/2018
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

32802×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3352×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

38702×

708NOENGL

Required label or labeling has been determined to not be in English in violation of 21 C.F.R. 201.15(c)(1).

752×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
7/10/2018
64AAL99DISINFECTANT N.E.C.
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
335LACKS N/C
3870708NOENGL
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/10/2018
64AAL99DISINFECTANT N.E.C.
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
335LACKS N/C
3870708NOENGL
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is INSTITUT KATHAROS's FDA import refusal history?

INSTITUT KATHAROS (FEI: 3014034786) has 2 FDA import refusal record(s) in our database, spanning from 7/10/2018 to 7/10/2018.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. INSTITUT KATHAROS's FEI number is 3014034786.

What types of violations has INSTITUT KATHAROS received?

INSTITUT KATHAROS has been cited for 6 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about INSTITUT KATHAROS come from?

All FDA import refusal data for INSTITUT KATHAROS is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.